ZipRecruiter

Log In

1

Analytical Method Development Jobs (NOW HIRING)

Iambic Therapeutics, Inc

$224K - $310K/yr

Lead analytical method development, validation, transfer, lifecycle management, and troubleshooting across DS and DP, ensuring methods are fit for purpose, scientifically sound, and aligned with ...

Abbott

Method Development Scientist

Santa Rosa, CA · On-site

$90K - $180K/yr

Career development with an international company where you can grow the career you dream of ... Troubleshoot existing analytical methods * Author, review, and verify validation protocols and ...

Abbott

Method Development Scientist

Santa Rosa, CA · On-site

$90K - $180K/yr

Career development with an international company where you can grow the career you dream of ... Troubleshoot existing analytical methods * Author, review, and verify validation protocols and ...

previous pagenext page

Showing results 21-40

All JobsTechnology JobsAnalytical Method Development Jobs

Analytical Method Development information

See salary details

$89K

$191.4K

$287.5K

How much do analytical method development jobs pay per year?

As of Sep 10, 2026, the average yearly pay for analytical method development in the United States is $191,412.00, according to ZipRecruiter salary data. Most workers in this role earn between $94,000.00 and $249,000.00 per year, depending on experience, location, and employer.

What is an analytical method development?

An Analytical Method Development job involves designing, optimizing, and validating methods for analyzing pharmaceutical, chemical, or biological samples. Professionals in this role ensure accurate, reliable, and reproducible results by developing techniques like chromatography, spectroscopy, or titration. They collaborate with research, quality control, and regulatory teams to comply with industry standards and guidelines. This role is critical in drug development, manufacturing, and ensuring product quality and safety.

What does an analytical method development do?

A typical day involves designing, executing, and optimizing analytical experiments to develop new testing methods or improve existing ones, often using advanced laboratory instruments. You may also analyze data, document results, troubleshoot instrument or methodological issues, and collaborate with scientists, quality assurance, and production teams. Regular tasks include preparing reports for regulatory submissions, participating in team meetings to discuss progress and challenges, and maintaining rigorous documentation standards. The role balances independent technical work with teamwork and cross-departmental communication to ensure methods meet performance, accuracy, and compliance standards.

What are the key skills and qualifications needed to thrive in analytical method development?

To excel in Analytical Method Development, a strong background in chemistry, analytical techniques, and statistical analysis is typically required, often supported by a relevant science degree. Familiarity with laboratory instrumentation such as HPLC, GC, MS, and validation protocols, as well as experience with software like Empower or ChemStation, is highly valued. Attention to detail, problem-solving, and effective communication are crucial soft skills for this role. These competencies are vital to ensure robust method development, regulatory compliance, and effective teamwork in a laboratory setting.

More about Analytical Method Development jobs

What are the most commonly searched types of Analytical Method Development jobs?

The most popular types of Analytical Method Development jobs are:

What states have the most Analytical Method Development jobs?

States with the most job openings for Analytical Method Development jobs include:

Analytical Method Development jobs near you
Infographic showing various Analytical Method Development job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, and 2% Contract. Highlights an 86% Physical, 3% Hybrid, and 11% Remote job distribution, with an average salary of $191,412 per year, or $92 per hour.

Director, Analytical Development

Cambridge, MA • On-site

Scorpion Therapeutics
51 - 200 employees
Learn more about Scorpion Therapeuticsexternal

$185K - $240K/yr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 5 days ago

Job description

Responsibilities:
  • Lead analytical development strategy, priorities, roadmap; develop phase-appropriate, risk-based analytical assays and potency testing for iPSC-derived cell therapy products.
  • Recruit/manage/train/mentor Analytical Development staff.
  • Lead analytical development and method transfer to support iPSC expansion/differentiation in GMP manufacturing across the product lifecycle.
  • Oversee development/authoring/review/approval of SOPs, test methods, and qualification documentation supporting GMP and QC.
  • Act as SME for analytical development; lead technology transfer (in-process, release, product characterization) to CDMOs and CTLs.
  • Resolve complex QC testing issues during clinical production at CDMOs (person-in-plant support as needed).
  • Develop/review/approve analytical development source documents; provide CMC oversight for regulatory submissions; support regulatory responses and influence analytical strategy.
  • Lead CTL due diligence, evaluation, and selection; support CDMO selection due diligence.
  • Drive continuous improvement; support budget/resource/capital planning.
  • Partner cross-functionally (Regulatory, Quality, CDMOs, CTLs, R&D) and perform other assigned duties.
Minimum requirements:
  • 15+ years (BS) OR 13+ years (MS) OR 10+ years (PhD) biotech/pharma experience in cell/gene therapy; 7+ years managerial experience.
  • Expertise in cell therapy analytical methods (potency assays, flow cytometry-based assays, product characterization); method development/optimization/qualification/transfer.
  • Hands-on characterization (flow cytometry, RT-PCR, ddPCR); safety assays for lot release (endotoxin, mycoplasma, sterility, rapid release).
  • Analytical control strategies/specifications; stability studies per ICH and shelf-life setting.
  • Potency assay development/strategy for cell therapy; experience with CDMOs/CTLs.
  • Regulatory/CMC filings experience; strong analytical/problem-solving, communication/technical writing/presentation, urgency/accountability, teamwork, and cross-functional collaboration.
Preferred qualifications:
  • PhD/MS in relevant fields; iPSC-derived analytical method development/qualification experience.
  • Whole genome sequencing, bioinformatics pipeline, scRNA-seq experience.
Compensation/benefits:
  • Salary range: $185,000-$240,000.
  • Comprehensive benefits (medical/dental/vision/prescription, wellness resources, 401k/ESPP, paid time off & paid parental leave, disability, etc.).
#J-18808-Ljbffr

Apply